Skip Navigation
ChemIDplus A TOXNET DATABASE LiteBrowseAdvanced

Substance Name: Phenomycin
RN: 12624-22-5
InChIKey: VEBJYUPFGABFPY-MSGKFRKUSA-N

Note

  • Isolated from Streptomyces fervens.

Classification Codes

  • Drug / Therapeutic Agent
  • Natural Product

Molecular Formula

  • C414-H667-N125-O129-S2

Molecular Weight

  • 9523.7013
 
* denotes mobile formatted website

Links to Resources

NLM Resources (File Locators)

Other Resources (Internet Locators)


Search for this InChIKey on the Web

Names and Synonyms

Name of Substance

  • Phenomycin

Systematic Name

  • Phenomycin

Registry Numbers

CAS Registry Number

  • 12624-22-5

System Generated Number

  • 0012624225

Structure Descriptors

InChI

1S/C414H667N125O129S2/c1-49-199(19)315(396(653)510-279(170-311(581)582)380(637)534-324(225(45)553)404(661)514-282(410(667)668)156-231-171-447-241-89-57-56-88-239(231)241)522-302(565)178-449-343(600)259(126-146-669-47)492-401(658)321(222(42)550)532-361(618)250(98-66-76-136-423)477-334(591)211(31)459-331(588)208(28)469-381(638)284(181-541)519-373(630)270(159-234-174-441-190-454-234)509-393(650)312(196(13)14)524-342(599)219(39)468-366(623)271(162-298(429)561)502-371(628)267(155-230-112-118-238(557)119-113-230)501-372(629)269(158-233-173-440-189-453-233)494-341(598)218(38)471-395(652)316(200(20)50-2)527-387(644)289(186-546)518-359(616)260(127-147-670-48)489-378(635)277(168-309(577)578)506-383(640)285(182-542)515-356(613)249(97-65-75-135-422)481-350(607)247(95-63-73-133-420)483-376(633)275(166-307(573)574)504-352(609)244(92-60-70-130-417)475-337(594)217(37)470-389(646)291-104-83-143-537(291)407(664)280(151-195(11)12)512-354(611)248(96-64-74-134-421)480-349(606)246(94-62-72-132-419)482-375(632)274(165-306(571)572)496-339(596)215(35)465-347(604)256(120-123-295(426)558)486-351(608)254(102-80-140-445-413(435)436)484-369(626)266(152-227-86-54-53-55-87-227)500-358(615)258(122-125-304(567)568)488-377(634)276(167-308(575)576)505-353(610)252(100-78-138-443-411(431)432)478-335(592)212(32)458-327(584)204(24)457-330(587)207(27)466-364(621)261(148-192(5)6)497-368(625)263(150-194(9)10)498-384(641)288(185-545)521-400(657)319(220(40)548)523-303(566)179-451-344(601)264(153-228-108-114-236(555)115-109-228)499-385(642)287(184-544)520-394(651)313(197(15)16)525-391(648)294-107-85-145-539(294)409(666)314(198(17)18)526-379(636)278(169-310(579)580)511-403(660)322(223(43)551)531-360(617)242(90-58-68-128-415)473-300(563)177-450-345(602)268(157-232-172-439-188-452-232)508-398(655)317(201(21)51-3)528-392(649)293-106-84-144-538(293)408(665)281(160-235-175-442-191-455-235)513-386(643)286(183-543)516-355(612)245(93-61-71-131-418)476-333(590)210(30)460-332(589)209(29)472-399(656)320(221(41)549)530-363(620)255(103-81-141-446-414(437)438)485-382(639)283(180-540)474-301(564)176-448-326(583)203(23)462-367(624)273(164-305(569)570)495-340(597)216(36)467-365(622)262(149-193(7)8)507-402(659)323(224(44)552)535-388(645)290(187-547)517-357(614)253(101-79-139-444-412(433)434)479-336(593)214(34)464-348(605)257(121-124-296(427)559)487-374(631)272(163-299(430)562)503-370(627)265(154-229-110-116-237(556)117-111-229)493-338(595)213(33)461-328(585)205(25)456-329(586)206(26)463-346(603)243(91-59-69-129-416)491-397(654)318(202(22)52-4)529-405(662)325(226(46)554)533-362(619)251(99-67-77-137-424)490-390(647)292-105-82-142-536(292)406(663)240(425)161-297(428)560/h53-57,86-89,108-119,171-175,188-226,240,242-294,312-325,447,540-557H,49-52,58-85,90-107,120-170,176-187,415-425H2,1-48H3,(H2,426,558)(H2,427,559)(H2,428,560)(H2,429,561)(H2,430,562)(H,439,452)(H,440,453)(H,441,454)(H,442,455)(H,448,583)(H,449,600)(H,450,602)(H,451,601)(H,456,586)(H,457,587)(H,458,584)(H,459,588)(H,460,589)(H,461,585)(H,462,624)(H,463,603)(H,464,605)(H,465,604)(H,466,621)(H,467,622)(H,468,623)(H,469,638)(H,470,646)(H,471,652)(H,472,656)(H,473,563)(H,474,564)(H,475,594)(H,476,590)(H,477,591)(H,478,592)(H,479,593)(H,480,606)(H,481,607)(H,482,632)(H,483,633)(H,484,626)(H,485,639)(H,486,608)(H,487,631)(H,488,634)(H,489,635)(H,490,647)(H,491,654)(H,492,658)(H,493,595)(H,494,598)(H,495,597)(H,496,596)(H,497,625)(H,498,641)(H,499,642)(H,500,615)(H,501,629)(H,502,628)(H,503,627)(H,504,609)(H,505,610)(H,506,640)(H,507,659)(H,508,655)(H,509,650)(H,510,653)(H,511,660)(H,512,611)(H,513,643)(H,514,661)(H,515,613)(H,516,612)(H,517,614)(H,518,616)(H,519,630)(H,520,651)(H,521,657)(H,522,565)(H,523,566)(H,524,599)(H,525,648)(H,526,636)(H,527,644)(H,528,649)(H,529,662)(H,530,620)(H,531,617)(H,532,618)(H,533,619)(H,534,637)(H,535,645)(H,567,568)(H,569,570)(H,571,572)(H,573,574)(H,575,576)(H,577,578)(H,579,580)(H,581,582)(H,667,668)(H4,431,432,443)(H4,433,434,444)(H4,435,436,445)(H4,437,438,446)/t199-,200-,201-,202-,203-,204-,205-,206-,207-,208-,209-,210-,211-,212-,213-,214-,215-,216-,217-,218-,219-,220+,221+,222+,223+,224+,225+,226+,240-,242-,243-,244-,245-,246-,247-,248-,249-,250-,251-,252-,253-,254-,255-,256-,257-,258-,259-,260-,261-,262-,263-,264-,265-,266-,267-,268-,269-,270-,271-,272-,273-,274-,275-,276-,277-,278-,279-,280-,281-,282-,283-,284-,285-,286-,287-,288-,289-,290-,291-,292-,293-,294-,312-,313-,314-,315-,316-,317-,318-,319-,320-,321-,322-,323-,324-,325-/m0/s1

InChIKey

VEBJYUPFGABFPY-MSGKFRKUSA-N

Smiles

CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](Cc1c[nH]c2c1cccc2)C(=O)O)NC(=O)CNC(=O)[C@H](CCSC)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cnc[nH]3)NC(=O)[C@H](C(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](Cc4ccc(cc4)O)NC(=O)[C@H](Cc5cnc[nH]5)NC(=O)[C@H](C)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](CO)NC(=O)[C@H](CCSC)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@@H]6CCCN6C(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](Cc7ccccc7)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H]([C@@H](C)O)NC(=O)CNC(=O)[C@H](Cc8ccc(cc8)O)NC(=O)[C@H](CO)NC(=O)[C@H](C(C)C)NC(=O)[C@@H]9CCCN9C(=O)[C@H](C(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CCCCN)NC(=O)CNC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@H](C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CO)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](Cc1ccc(cc1)O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCCCN)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CCCCN)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(=O)N)N

Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 subcutaneous 8mg/kg (8mg/kg)   Journal of Antibiotics. Vol. 21, Pg. 106, 1968.
mouse LDLo intraperitoneal 20ug/kg (0.02mg/kg)   "Antibiotics: Origin, Nature, and Properties," Korzyoski, T., et al., eds., Washington, DC, American Soc. for Microbiology, 1978Vol. 2, Pg. 1417, 1978.